James Sutcliffe
Last active: 2/20/2014

  1. Genome-wide linkage analyses of quantitative and categorical autism subphenotypes. Liu XQ, Paterson AD, Szatmari P, Autism Genome Project Consortium (2008) Biol Psychiatry 64(7): 561-70
    › Primary publication · 18632090 (PubMed) · PMC2670970 (PubMed Central)
  2. Genetics. Insights into the pathogenesis of autism. Sutcliffe JS (2008) Science 321(5886): 208-9
    › Primary publication · 18621658 (PubMed)
  3. Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder. Campbell DB, Li C, Sutcliffe JS, Persico AM, Levitt P (2008) Autism Res 1(3): 159-68
    › Primary publication · 19360663 (PubMed) · PMC2678909 (PubMed Central)
  4. Affiliative behaviors and beyond: it's the phenotype, stupid. Sutcliffe JS (2008) Biol Psychiatry 63(10): 909-10
    › Primary publication · 18452756 (PubMed)
  5. Strong association of de novo copy number mutations with autism. Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, Walsh T, Yamrom B, Yoon S, Krasnitz A, Kendall J, Leotta A, Pai D, Zhang R, Lee YH, Hicks J, Spence SJ, Lee AT, Puura K, Lehtimäki T, Ledbetter D, Gregersen PK, Bregman J, Sutcliffe JS, Jobanputra V, Chung W, Warburton D, King MC, Skuse D, Geschwind DH, Gilliam TC, Ye K, Wigler M (2007) Science 316(5823): 445-9
    › Primary publication · 17363630 (PubMed) · PMC2993504 (PubMed Central)
  6. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Autism Genome Project Consortium, Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, Feuk L, Qian C, Bryson SE, Jones MB, Marshall CR, Scherer SW, Vieland VJ, Bartlett C, Mangin LV, Goedken R, Segre A, Pericak-Vance MA, Cuccaro ML, Gilbert JR, Wright HH, Abramson RK, Betancur C, Bourgeron T, Gillberg C, Leboyer M, Buxbaum JD, Davis KL, Hollander E, Silverman JM, Hallmayer J, Lotspeich L, Sutcliffe JS, Haines JL, Folstein SE, Piven J, Wassink TH, Sheffield V, Geschwind DH, Bucan M, Brown WT, Cantor RM, Constantino JN, Gilliam TC, Herbert M, Lajonchere C, Ledbetter DH, Lese-Martin C, Miller J, Nelson S, Samango-Sprouse CA, Spence S, State M, Tanzi RE, Coon H, Dawson G, Devlin B, Estes A, Flodman P, Klei L, McMahon WM, Minshew N, Munson J, Korvatska E, Rodier PM, Schellenberg GD, Smith M, Spence MA, Stodgell C, Tepper PG, Wijsman EM, Yu CE, Rogé B, Mantoulan C, Wittemeyer K, Poustka A, Felder B, Klauck SM, Schuster C, Poustka F, Bölte S, Feineis-Matthews S, Herbrecht E, Schmötzer G, Tsiantis J, Papanikolaou K, Maestrini E, Bacchelli E, Blasi F, Carone S, Toma C, Van Engeland H, de Jonge M, Kemner C, Koop F, Koop F, Langemeijer M, Langemeijer M, Hijmans C, Hijimans C, Staal WG, Baird G, Bolton PF, Rutter ML, Weisblatt E, Green J, Aldred C, Wilkinson JA, Pickles A, Le Couteur A, Berney T, McConachie H, Bailey AJ, Francis K, Honeyman G, Hutchinson A, Parr JR, Wallace S, Monaco AP, Barnby G, Kobayashi K, Lamb JA, Sousa I, Sykes N, Cook EH, Guter SJ, Leventhal BL, Salt J, Lord C, Corsello C, Hus V, Weeks DE, Volkmar F, Tauber M, Fombonne E, Shih A, Meyer KJ (2007) Nat Genet 39(3): 319-28
    › Primary publication · 17322880 (PubMed) · PMC4867008 (PubMed Central)
  7. Contribution of SHANK3 mutations to autism spectrum disorder. Moessner R, Marshall CR, Sutcliffe JS, Skaug J, Pinto D, Vincent J, Zwaigenbaum L, Fernandez B, Roberts W, Szatmari P, Scherer SW (2007) Am J Hum Genet 81(6): 1289-97
    › Primary publication · 17999366 (PubMed) · PMC2276348 (PubMed Central)
  8. Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility. Weiss LA, Kosova G, Delahanty RJ, Jiang L, Cook EH, Ober C, Sutcliffe JS (2006) Eur J Hum Genet 14(8): 923-31
    › Primary publication · 16724005 (PubMed)
  9. Mutations in GABRA1, GABRA5, GABRG2 and GABRD receptor genes are not a major factor in the pathogenesis of familial focal epilepsy preceded by febrile seizures. Ma S, Abou-Khalil B, Blair MA, Sutcliffe JS, Haines JL, Hedera P (2006) Neurosci Lett 394(1): 74-8
    › Primary publication · 16256272 (PubMed)
  10. Lack of association between autism and SLC25A12. Rabionet R, McCauley JL, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS, Haines JL, DeLong GR, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Pericak-Vance MA (2006) Am J Psychiatry 163(5): 929-31
    › Primary publication · 16648338 (PubMed)